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Neurodiagnostics, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K843253
EMG/NCV & EVOKED RESPONSE, DESIGN W/
November 20, 1984
K830191
NEURO DIAGNOSTICS MODEL FCR
February 18, 1983
K801670
NDI-IKE EMG
August 4, 1980
K801671
ESG-1 (EVOKED RESPONSE STIMULUS GENER)
August 4, 1980